METFORMIN HYDROCHLORIDE
NDC 50228-589, METFORMIN HYDROCHLORIDE, tablet, from ScieGen Pharmaceuticals Inc.
- Product NDC
- 50228-589
- Status
- Listed
- Labeler
- ScieGen Pharmaceuticals Inc
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA203769
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/50228-589 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- METFORMIN HYDROCHLORIDE750 mg/1
Pharmacologic classes
Biguanide [EPC]; Biguanides [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 50228-589-05 | 50228058905 | 500 TABLET in 1 BOTTLE (50228-589-05) |
| 50228-589-30 | 50228058930 | 30 TABLET in 1 BOTTLE (50228-589-30) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/4e4c4ba9-65c6-4273-8f6b-2423ab521dad
Use it
Look up 50228-589 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/50228-589 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 50228-589. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.